Bärbel Dittrich - Concepedia

Author

Bärbel Dittrich

Essen University Hospital

Also Known As

B Dittrich, B. Dittrich, Bärbel Dittrich

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Essen University Hospital Institut für Medizinische Informatik, Biometrie und Epidemiologie Case Western Reserve University Humboldt-Universität zu Berlin Hadassah Academic College

About

Bärbel Dittrich is an author at Essen University Hospital specializing in genetics, medicine, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	1.2K
2	Molecular Biology	3	3	71
3	Molecular Genetics	3	3	654
4	Natural Sciences	1	1	37
5	Biochemistry	1	1	37

Bärbel Dittrich

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15 Karin Buiting, Shinji Saitoh, Bärbel Dittrich, Nature Genetics Developmental BiologyGenetic DisorderDevelopmental GeneticsGeneticsChromosome Biology	1995	598
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene Bärbel Dittrich, Karin Buiting, Bernd Korn, Nature Genetics ChromatinTranscriptional RegulationDevelopmental BiologyDevelopmental GeneticsGenetics	1996	257
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes. André Reis, Bärbel Dittrich, Valerie Greger, PubMed	1994	224
Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis Karin Buiting, Bärbel Dittrich, Stephanie Groß, The American Journal of Human Genetics Developmental AnomalyGenetic DisorderGeneticsSporadic Imprinting DefectsGynecology	1998	215
Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method Michael Zeschnigk, Birgit Schmitz, Bärbel Dittrich, Human Molecular Genetics	1997	140
Characterization of a methylation imprint in the Prader — Willi syndrome chromosome region Bärbel Dittrich, Karin Buiting, Stephanie Groß, Human Molecular Genetics	1993	85
Different Mechanisms and Recurrence Risks of Imprinting Defects in Angelman Syndrome Joachim Bürger, Karin Buiting, Bärbel Dittrich, The American Journal of Human Genetics Developmental AnomalyDifferent MechanismsAngelman SyndromeNeurogeneticsMedicine	1997	64
Detection of aberrant DNA methylation in unique Prader — Willi syndrome patients and its diagnostic implications Karin Buiting, Bärbel Dittrich, Wendy P. Robinson, Human Molecular Genetics	1994	48
Two Radish Genes for 3-Hydroxy-3-Methylglutaryl-CoA Reductase Isozymes Complement Mevalonate Auxotrophy in a Yeast Mutant and Yield Membrane-Bound Active Enzyme Kai‐Uwe Vollack, Bärbel Dittrich, Albert Ferrer, Journal of Plant Physiology BiosynthesisCellular EnzymologyBiochemistryNatural SciencesGenetics	1994	37
Identification of Novel Exons 3′ to the HumanSNRPNGene Karin Buiting, Bärbel Dittrich, Sabine Endele, Genomics Molecular GeneticsPrion DiseaseMolecular BiologyNovel Exons 3′	1997	19

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